Evidence map›Paper›PMID 29983235›Full record

ArticleJournal of pharmacological sciences2018

Effect of a SGLT2 inhibitor on the systemic and intrarenal renin-angiotensin system in subtotally nephrectomized rats.

Lei Li, Yoshio Konishi, Takashi Morikawa, Yifan Zhang, Chizuko Kitabayashi, Hideki Kobara, Tsutomu Masaki, Daisuke Nakano, Hirofumi Hitomi, Hiroyuki Kobori and 1 more

Abstract read
In one paragraph

Article in Journal of pharmacological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. New Insight in Cardiorenal Syndrome: From Biomarkers to Therapy.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Review
  15. SGLT2 inhibition effect on salt-induced hypertension, RAAS, and NaAmerican journal of physiology. Renal physiology · 2022
    Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Molecular Mechanisms of SGLT2 Inhibitor on Cardiorenal Protection.International journal of molecular sciences · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Lei LiDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Yoshio KonishiDivision of Nephrology and Hypertension, Osaka City General Hospital, Osaka, Japan.
Takashi MorikawaDivision of Nephrology and Hypertension, Osaka City General Hospital, Osaka, Japan.
Yifan ZhangDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Chizuko KitabayashiDivision of Nephrology and Hypertension, Osaka City General Hospital, Osaka, Japan.
Hideki KobaraDepartment of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Tsutomu MasakiDepartment of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Daisuke NakanoDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Hirofumi HitomiDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Hiroyuki KoboriDepartments of Pharmacology and Nephrology, School of Medicine, International University of Health and Welfare, Tokyo, Japan.
Akira NishiyamaDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: akira@kms.ac.jp.

Funding

Intrarenal Augmentation of Angiotensinogen by Ang IIR01DK072408 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI NAVAR, LUIS GABRIEL · 2006 to 2010
$1.2M
NIDDK NIH HHS R01 DK072408
6 · The paper itself

Abstract

We aimed to examine the effects of a sodium glucose co-transporter 2 (SGLT2) inhibitor on systemic and intrarenal renin-angiotensin system (RAS) in subtotally nephrectomized non-diabetic rats, a model of chronic kidney disease (CKD). Oral administration of the selective SGLT2 inhibitor, TA-1887 (10 mg/kg/day), for 10 weeks induced glycosuria. However, plasma renin activity, plasma angiotensinogen levels, kidney angiotensin II contents and renal injury were not significantly affected by TA-1887. These data indicate that chronic treatment with an SGLT2 inhibitor does not activate the systemic and intrarenal RAS in subjects with non-diabetic CKD.

Indexed as

Sodium-Glucose Transporter 2 InhibitorsAdministration, OralAngiotensin IIAngiotensinogenAnimalsDisease Models, AnimalGlucosidesGlycosuriaIndolesKidneyMaleNephrectomyRats, Sprague-DawleyRenal Insufficiency, ChronicReninRenin-Angiotensin SystemAngiotensin IIAngiotensinogenGlucosidesIndolesReninSlc5a2 protein, ratSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsChronic kidney disease (CKD)Renin–angiotensin system (RAS)SGLT2 inhibitor

Identifiers

PMID29983235
PMCPMC6050139

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.